Nitric oxide-releasing dendrimers for the treatment of periodontal disease
Nitric oxide-releasing dendrimers for the treatment of periodontal disease
批准号:
9261511
负责人:
Mark H Schoenfisch
金额:
$30.99万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-07-02 至 2020-04-30
关键词:
AdultAdverse effectsAerobicAnaerobic BacteriaAnti-Bacterial AgentsAnti-Inflammatory AgentsAnti-inflammatoryAntibioticsAwarenessBacteriaCaliberCardiovascular DiseasesCaringCellsCharacteristicsChargeChemicalsCystic FibrosisDendrimersDental CareDental PlaqueDiabetic Foot UlcerDiffusionEpidemicExpenditureForeign BodiesGenerationsGingivaGingivitisGoalsHalf-LifeHealthHealth ExpendituresHealthcare SystemsHeart DiseasesImmune responseIn VitroInfectionInflammationInnate Immune ResponseKineticsLocal Anti-Infective AgentsMalignant NeoplasmsMicrobial BiofilmsMicrobiologyModelingMolecular WeightMusNatureNitric OxideOralOral healthPathogenicityPenetrationPeriodontal DiseasesPeriodontal InfectionPeriodontal PocketPeriodontitisPhysiologicalPreventionPropertyResearchRisk FactorsRoleSafetyStrokeStructureSystemTestingTissuesWorkantimicrobialbactericidebasecombatcytotoxiccytotoxicitydesignefficacy studyin vitro Modelin vivokillingslipophilicitymicrobialmicrobial communitymolecular sizemouse modelnovel strategiesoral plaquepathogenperiodontopathogenpreventprogramspublic health relevanceresponsescaffoldsoft tissuesubcutaneoussubgingival biofilmsuccesstherapeutic development
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of this proposal is to develop nitric oxide releasing dendrimers to inhibit biofilm based periodontopathogens and associated periodontal disease. The rationale for pursuing this work is based on nitric oxide's broad spectrum antimicrobial activity, rapid diffusion through biofilms, short half-life (thus imparting local acton) and physiological role in the immune response to pathogens. The use of a macromolecular NO release scaffold enables us to maximize bactericidal activity while minimizing the cytotoxic impact on healthy oral cells and tissue. We will study the influence of dendrimer size/molecular weight, charge, exterior functionality, and NO release properties on pathogenic plaque bacteria killing. We will systematically study both dendrimer and nitric oxide penetration into in vitro models of oral plaque biofilms as a function of biofilm composition, maturity and mass. An established murine model for periodontal infection will be employed to evaluate how dendrimer composition and nitric oxide release influence inflammation, host immune response, and biofilm eradication.
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海外基金